Search results for " market"
Article
Aseptic Processing: Keeping it Safe
…terile products must have validated processes “of the same standard as for products authorized for marketing,” according to the European Commission’s EU Guidelines to Good Manufacturing Practice: Med…
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A Bright Future for the Plasma Fractionation Industry
There is also a vast difference between the developed and emerging markets. According to Perreault, there is a strong need for global policies and actions to support development, diagnosis, and treatm…
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New Era for Generic Drugs
…s seeking patent extensions and consumers demanding a clearer pathway for bringing low-cost drugs to market. Former FDA officials recalled the challenges in establishing new policies for testing and …
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Elucidating Biosimilars Characterization
The growth corresponds to a 20% increase from last year’s figures and accounts for approximately 2% of the overall biologics market. Although narrowly focused on only a small number of therapy areas a…
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What is process development?
Ultimately, you will need a process that translates to a manufacturing environment, one that is easy to scale up throughout clinical trials and to the market. By the time you reach Phase III in the dr…
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Report from the 12th Plasma Product Biotechnology Forum
The Future
The conference ended with a forward-looking session to address global trends in the plasma product market. From the presentations it can be concluded that the market has both a brigh…
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Track-and-Trace Progress Benefits Supply-Chain Security Efforts
Dubbing the new market “real-time transportation visibility platforms,” as opposed to track-and-trace technology, the tech market analysts at Gartner predict that, by 2023, half of all global product-…
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Remote Monitoring and Big Data Advance Upstream Automation
…, as are solutions that can be rapidly deployed and easily scaled, thus helping manufacturers get to market faster. A key component of those solutions, adds Chris Sandusky, director of automation sol…
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The Importance of Process Intensification and PAT for Achieving Real-Time Release
…rease efficiency and thereby reduce the cost of producing drugs and the time it takes to get them to market. Workflows, capital and operating expenses, product quality, and waste production can all b…
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Eliminating Residual Impurities Starts with a Strategic Plan
Other factors relate to the testing process itself, according to Lisa Sapp, biopharma market manager with Agilent Technologies. The selected isolation method—precipitation, filtration, centrifugation,…